MPJ — Interarticular Disc Prosthesis (Interpositional Implant) Class III

FDA Device Classification

FDA product code MPJ covers "Interarticular Disc Prosthesis (Interpositional Implant)", a Class III medical device regulated under 21 CFR 872.3970. Submissions are reviewed by the Dental panel. Devices under this code are implants.

Classification Details

Product Code
MPJ
Device Class
Class III
Regulation Number
872.3970
Submission Type
Review Panel
DE
Medical Specialty
Dental
Implant
Yes